Incidental Mutation 'R8400:Cutc'
ID 647840
Institutional Source Beutler Lab
Gene Symbol Cutc
Ensembl Gene ENSMUSG00000025193
Gene Name cutC copper transporter
Synonyms 2310039I18Rik, CGI-32
MMRRC Submission
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.342) question?
Stock # R8400 (G1)
Quality Score 225.009
Status Not validated
Chromosome 19
Chromosomal Location 43752996-43768638 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 43753205 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 15 (S15P)
Ref Sequence ENSEMBL: ENSMUSP00000107678 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026199] [ENSMUST00000045562] [ENSMUST00000112047] [ENSMUST00000153295]
AlphaFold Q9D8X1
Predicted Effect probably benign
Transcript: ENSMUST00000026199
AA Change: S15P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000026199
Gene: ENSMUSG00000025193
AA Change: S15P

DomainStartEndE-ValueType
Pfam:CutC 25 216 1.1e-71 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000045562
SMART Domains Protein: ENSMUSP00000041820
Gene: ENSMUSG00000040018

DomainStartEndE-ValueType
Pfam:COX15-CtaA 73 402 2.3e-112 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000112047
AA Change: S15P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000107678
Gene: ENSMUSG00000025193
AA Change: S15P

DomainStartEndE-ValueType
Pfam:CutC 25 226 7.8e-81 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000153295
AA Change: S15P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000118906
Gene: ENSMUSG00000025193
AA Change: S15P

DomainStartEndE-ValueType
Pfam:CutC 23 224 7.7e-82 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the CUT family of copper transporters are associated with copper homeostasis and are involved in the uptake, storage, delivery, and efflux of copper (Gupta et al., 1995 [PubMed 7635807]; Li et al., 2005 [PubMed 16182249]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 G A 11: 9,293,925 M1929I probably benign Het
Abca13 T C 11: 9,298,218 I2655T probably damaging Het
Acad10 A G 5: 121,626,205 V887A possibly damaging Het
Acot10 T C 15: 20,666,172 E161G possibly damaging Het
Astn1 C T 1: 158,657,100 P919L probably benign Het
Atp1a4 T A 1: 172,234,494 D688V probably damaging Het
C4bp C A 1: 130,636,747 C400F probably damaging Het
Col6a6 A C 9: 105,774,796 D1005E probably damaging Het
Csnk1g3 C T 18: 53,953,288 R422C probably benign Het
Dgkb T C 12: 38,602,838 probably null Het
Disc1 T C 8: 125,232,993 V748A probably benign Het
Dmbt1 C G 7: 131,082,587 D778E unknown Het
Dmxl2 T C 9: 54,383,753 Y2471C probably benign Het
Fam185a T A 5: 21,438,816 N243K probably benign Het
Fchsd2 A T 7: 101,253,573 Q386L possibly damaging Het
Gm904 C A 13: 50,643,417 P49Q probably damaging Het
H2-Q10 C T 17: 35,470,477 R59C probably damaging Het
Ier5l A G 2: 30,473,093 Y307H possibly damaging Het
Kmt2e C A 5: 23,497,092 T906K probably benign Het
Kndc1 C T 7: 139,913,518 R467W probably damaging Het
Muc5ac C A 7: 141,810,476 T2508K probably damaging Het
Nlrp9a A T 7: 26,565,006 M784L probably benign Het
Nlrp9b T A 7: 20,024,012 C391* probably null Het
Nubp2 A C 17: 24,884,465 M146R probably damaging Het
Olfr1295 A T 2: 111,565,402 L14H probably damaging Het
Olfr1359 G A 13: 21,703,915 V305M probably benign Het
Olfr1419 T A 19: 11,871,214 M1L probably damaging Het
Olfr43 C T 11: 74,206,395 V274M possibly damaging Het
Olfr694 T A 7: 106,689,669 S21C probably benign Het
Olfr857 A T 9: 19,713,093 N89Y probably benign Het
Otud1 T C 2: 19,658,378 V106A possibly damaging Het
Pcdhac1 T A 18: 37,092,400 Y755* probably null Het
Pkd1l3 C T 8: 109,623,888 P455L possibly damaging Het
Ptprb GAGACCCTCGGGAGCACTGCAGAGACCCTCAGGAACACTGCAAAGACCCTCGGGAGCACTGCAGAGACCCTCAGGAACACTGCAAAGACCCTCGGGAGCACTGCAGAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACT GAGACCCTCGGGAGCACTGCAGAGACCCTCAGGAACACTGCAAAGACCCTCGGGAGCACTGCAGAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACT 10: 116,283,572 probably benign Het
Samhd1 T C 2: 157,099,433 E648G probably benign Het
Smarca5 T C 8: 80,709,127 T794A probably benign Het
Spc24 A T 9: 21,757,730 L87H probably damaging Het
Sppl2b TGTCACAGGT TGT 10: 80,866,069 probably null Het
Stra6l G A 4: 45,864,905 R77Q probably damaging Het
Tdrd1 G A 19: 56,848,649 V472M probably benign Het
Tsc2 A T 17: 24,604,987 I948K possibly damaging Het
Ttc39d T C 17: 80,216,005 V31A probably benign Het
Vmn1r158 A T 7: 22,789,880 C301* probably null Het
Vmn2r22 A T 6: 123,637,527 L368* probably null Het
Vmn2r79 A G 7: 87,002,100 T236A probably benign Het
Vwa1 T C 4: 155,772,768 H191R probably benign Het
Zdbf2 T A 1: 63,304,976 V838E possibly damaging Het
Other mutations in Cutc
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03245:Cutc APN 19 43768182 missense possibly damaging 0.83
P0028:Cutc UTSW 19 43764969 missense possibly damaging 0.84
PIT4305001:Cutc UTSW 19 43768269 missense probably damaging 0.99
R0095:Cutc UTSW 19 43753199 missense probably benign
R0479:Cutc UTSW 19 43768216 missense probably damaging 1.00
R5635:Cutc UTSW 19 43755630 missense probably benign 0.09
R5898:Cutc UTSW 19 43760029 missense probably benign 0.00
R6150:Cutc UTSW 19 43759889 missense probably damaging 1.00
R6217:Cutc UTSW 19 43759997 missense probably damaging 0.99
R6392:Cutc UTSW 19 43760050 missense possibly damaging 0.58
R7573:Cutc UTSW 19 43759943 missense probably benign 0.03
R8817:Cutc UTSW 19 43755674 missense probably benign 0.33
R9133:Cutc UTSW 19 43767288 missense possibly damaging 0.93
R9789:Cutc UTSW 19 43768260 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- AGAACAAGCACTTCCGGGTC -3'
(R):5'- TTATCTACCACAGAGACAGGGAGG -3'

Sequencing Primer
(F):5'- TAGGTTGGCCACTGCGC -3'
(R):5'- TGAGGGCACTTGCGAGACTG -3'
Posted On 2020-09-02